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CAS

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107447-06-3

(3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate is a complex ester derivative of tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid, featuring a methyl group on the carboxyl group, and isobutyl and methoxy groups attached to the nitrogen and carbon atoms, respectively. This molecule may possess potential biological activity or therapeutic applications, but further research is required to ascertain its specific properties and uses.

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  • (3S)-methyl 1-isobutyl-7-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate

    Cas No: 107447-06-3

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  • 107447-06-3 Structure

  • Basic information

    1. Product Name: (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
    2. Synonyms: (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
    3. CAS NO:107447-06-3
    4. Molecular Formula: C18H24N2O3
    5. Molecular Weight: 316.39476
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107447-06-3.mol

  • Chemical Properties

    1. Melting Point: 151-153.5 °C
    2. Boiling Point: 472.7±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.140±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 17.46±0.60(Predicted)
    10. CAS DataBase Reference: (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(107447-06-3)
    12. EPA Substance Registry System: (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(107447-06-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 107447-06-3(Hazardous Substances Data)

107447-06-3 Usage

Uses

As the provided materials do not specify any particular applications for (3S)-Methyl 1-isobutyl-7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate, it is not possible to list its uses based on the given information. However, given its structural complexity and the presence of various functional groups, it could potentially be explored for applications in pharmaceuticals, agrochemicals, or other industries where novel compounds with unique properties are sought. Further research and testing would be necessary to determine its specific applications and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 107447-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107447-06:
(8*1)+(7*0)+(6*7)+(5*4)+(4*4)+(3*7)+(2*0)+(1*6)=113
113 % 10 = 3
So 107447-06-3 is a valid CAS Registry Number.

107447-06-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (1R,3S)-7-methoxy-1-(2-methylpropyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names (1R,3S)-METHYL 1-ISOBUTYL-7-METHOXY-2,3,4,9-TETRAHYDRO-1H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107447-06-3 SDS

107447-06-3Downstream Products

107447-06-3Relevant articles and documents

Synthetic Approaches to Fumitremorgins. III. Synthesis of Optically Active Pentacyclic Ring Systems, and Their Oxidation at Ring C

Nakagawa, Masako,Fukushima, Hiroshi,Kawate, Tomohiko,Hongu, Mitsuya,Une, Teruaki,et al.

, p. 23 - 32 (2007/10/02)

Pictet-Spengler reaction of L-tryptophan methyl ester (9) and 6-methoxy-L-tryptophan methyl ester (40) with isovaleraldehyde (10) in methylene chloride in the presence of trifluoroacetic acid gave the cis-tetrahydro-β-carboline (11, 41) as the major isome

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